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Baumgartner M

References (2)

Title : Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report - De Gier_2022_Atherosclerosis_355_65
Author(s) : De Gier C , Skacel G , Walleczek NK , Lischka J , Baumgartner M , Greber-Platzer S
Ref : Atherosclerosis , 355 :65 , 2022
Abstract :
PubMedSearch : De Gier_2022_Atherosclerosis_355_65
PubMedID:
Gene_locus related to this paper: human-LPL

Title : The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study - Krenn_2022_J.Neurol__
Author(s) : Krenn M , Sener M , Rath J , Zulehner G , Keritam O , Wagner M , Laccone F , Iglseder S , Marte S , Baumgartner M , Eisenkolbl A , Liechtenstein C , Rudnik S , Quasthoff S , Grinzinger S , Spenger J , Wortmann SB , Loscher WN , Zimprich F , Kellersmann A , Rappold M , Bernert G , Freilinger M , Cetin H
Ref : Journal of Neurology , : , 2022
Abstract :
PubMedSearch : Krenn_2022_J.Neurol__
PubMedID: 36308527